BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Ophthalmic Sealant

    PMA: P130004 · Supplement: S002 · Decision Jul 21, 2016
    View on FDA
    Classifications
    1
    FEI Numbers
    2
    Registration Numbers
    2

    Basic Information

    Device Name
    Ophthalmic Sealant
    Trade Name
    RESURE SEALANT
    PMA Number
    P130004
    Supplement Number
    S002
    Device Class
    FDA Class 3
    Product Code
    PFZ
    Generic Name
    Ophthalmic Sealant
    Medical Specialty
    Unknown
    Advisory Committee
    Ophthalmic
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    July 21, 2016
    Date Received
    February 7, 2014
    Supplement Type
    Normal 180 Day Track No User Fee
    Supplement Reason
    Postapproval Study Protocol - OSB
    Expedited Review
    N

    Advisory Committee Statement

    Approval for the ReSure® Sealant Device Exposure Registry post-approval study protocol.

    Classifications

    This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    PFZ Ophthalmic Sealant